Medical Devices Solutions

PROLIM PLM software solutions enable managing product knowledge across the organization. Our solutions are trusted by medical equipment, and are regulatory, engineering, and content and document management compliant.

Competition, rules, expenses, and organizational complexities intensify the risks involved. It is better to prepare well to weather the storm. Not only building the right product, but building it right as well is of paramount importance. To achieve this feat, decisions should be made on basis:

  • Integrating cross-domain knowledge into a central, logical source that is accessible for everyone, everywhere in the business.
  • Enabling decision-makers to make more unified choices with others while being aware of how their choices affect people across the enterprise, even if it’s how mechanical design affects electronics.
  • Electronics design impacting software; or the ripple effect of a change throughout the entire system.
  • Enabling cross-functional knowledge sharing and providing people the information they need to act as swiftly as possible.
  • A solid PLM system is the best approach to retain control and make smarter decisions for development, manufacturing, and quality processes.

Meeting medical Equipment Industry challenges –

The process of making a medical equipment has always been complex, and full of interconnected procedures. The medical equipment industries is expected to effectively manage the immensely complex product development processes. Meanwhile, its always a challenge to address issues like:

  • Regulatory requirements
  • Systems engineering
  • Risk management
  • Competition
  • Increasing costs

PROLIM PLM Software’s suite of product lifecycle management solutions is comprehensive. It allows medical equipment manufacturers to obtain proper control, predictable project schedule and budgets, with competitive capability and performance.

  • World-class features and functionalities integrated into engineering tools to facilitate effective product and process development even in a multi-CAD environment.
  • Mitigates risk and facilitates re-use for future goods. Allows for document controls and lifecycle traceability, integrating workflows and deliverables from R&D, production, quality, services, and regulatory. 
  • Predictable design control, connecting deadlines and deliverables to the actual execution of the workflow. Also, validating and verifying outputs.

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